Product NDC: | 17856-0608 |
Proprietary Name: | Promethazine Hydrochloride |
Non Proprietary Name: | Promethazine Hydrochloride |
Active Ingredient(s): | 6.25 mg/5mL & nbsp; Promethazine Hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | SYRUP |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17856-0608 |
Labeler Name: | Atlantic Biologicals Corps |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA087953 |
Marketing Category: | ANDA |
Start Marketing Date: | 19821115 |
Package NDC: | 17856-0608-5 |
Package Description: | 5 mL in 1 CUP (17856-0608-5) |
NDC Code | 17856-0608-5 |
Proprietary Name | Promethazine Hydrochloride |
Package Description | 5 mL in 1 CUP (17856-0608-5) |
Product NDC | 17856-0608 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Promethazine Hydrochloride |
Dosage Form Name | SYRUP |
Route Name | ORAL |
Start Marketing Date | 19821115 |
Marketing Category Name | ANDA |
Labeler Name | Atlantic Biologicals Corps |
Substance Name | PROMETHAZINE HYDROCHLORIDE |
Strength Number | 6.25 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Phenothiazine [EPC],Phenothiazines [Chemical/Ingredient] |